Translation for '
autosomal' from English to Russian
ADJ positive | comparative | superlative
1 translation
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Usage Examples English
- RGR-opsin may be associated with autosomal recessive and autosomal dominant retinitis pigmentosa (arRP and adRP, respectively).
- Some examples are Down syndrome (aneuploidy), Usher syndrome (autosomal recessive), Treacher Collins syndrome (autosomal dominant), Crouzon syndrome (autosomal dominant), and Alport syndrome (X-linked).
- Emery–Dreifuss muscular dystrophy can be sub-classified by pattern of inheritance: X-linked, autosomal dominant, and autosomal recessive.
- ... not located on the X chromosome) are considered autosomal.
- Of the cystic kidney diseases, the most common is polycystic kidney disease with two sub-types: the less prevalent autosomal recessive and more prevalent autosomal dominant.
- It is either autosomal recessive or autosomal dominant.
- Primary auto-immune ataxias (PACA) lack diagnostic biomarkers. Cerebellar ataxias can be classified as sporadic, autosomal recessive, X-linked, autosomal dominant and of mitochondrial origin.
- Cone dystrophy in general usually occurs sporadically. Hereditary forms are usually autosomal dominant, and instances of autosomal recessive and X-linked inheritance also occur.
- Two forms of inheritance pattern for bifid noses have been described: autosomal recessive and autosomal dominant.
- There is a less common, autosomal dominant form, which is milder than the autosomal recessive forms, ranging from no symptoms to wheel chair dependence after age 60.
- Mutations in the "CLCN7" gene are responsible for about 75 percent of cases of autosomal dominant osteopetrosis, 10 to 15 percent of cases of autosomal recessive osteopetrosis, and all known cases of intermediate autosomal osteopetrosis.
- Hereditary spherocytosis can be an autosomal recessive or autosomal dominant trait.
- Mutations in this gene are associated with autosomal recessive neurosensory deafness, autosomal dominant sensorineural deafness without vestibular involvement, and DFNB36.
- The inheritance pattern is autosomal, but there are arguments as to whether it is autosomal dominant or autosomal recessive.
- The inheritance of Kyrle disease is unknown as reported cases point to both autosomal dominance and autosomal recessiveness.
- File:Autosomal dominant - en.svg|This condition is inherited in an autosomal dominant manner.
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Contains translations by TU Chemnitz and Mr Honey's Business Dictionary (German-English only).
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